Mobile rapid test system for nucleic acid analysis

ABSTRACT

A mobile rapid test system for nucleic acid analysis. A method comprising the steps of amplification of the nucleic acids by means of rapid-PCR technology, conversion of a double-stranded amplification product into a single-stranded DNA fragment, hybridization with a labeled probe and detection of the nucleic acids on a lateral-flow test strip. A device comprising a reaction cavity which preferably consists of a thin film, inlet and outlet openings for the reaction cavity, one or more heatable sample blocks which are connected to miniaturized cooling bodies and a window for reading off the result. The lateral-flow test strip is a component of the mobile rapid test system. Operation of the instrument system requires no external power source, but only batteries or a rechargeable battery.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit under 35 U.S.C. §365(c) and 35 U.S.C.§120 to PCT/EP2008/068197, filed Dec. 22, 2008, which claims priority toGermany 10 2007 062 441.9, filed Dec. 22, 2007. Both of these documentsare hereby incorporated by reference in their entireties.

BACKGROUND OF THE INVENTION

1. Field of the Invention

A mobile equipment system for gene diagnostics.

2. Description of the Related Art

The examination of diagnostically relevant biological samples, such asserum, plasma, blood, swab samples, or organ smears, for the detectionof infectious pathogens has gained tremendous importance in recentyears. Viral infections such as HIV, HCV, or HBV are increasingworldwide. Furthermore, bacterial infections are also increasing again,among other things also as the result of climatic changes. Theoccurrence of new, deadly infectious diseases having an extremely highinfection potential (SARS, bird flu) shows more and more clearly thatrapid diagnostics, which can be carried out on site, are decisive forpreventing epidemics. Furthermore, diagnostic systems that are easy tohandle and relatively inexpensive also play an important role,particularly for developing countries, in combating the spread ofinfectious diseases. The majority of the tests currently being usedprimarily for the detection of viral infectious diseases (HIV, HCV, HBV)are based on carrying out REAL-TIME PCRs. These tests are tied toextremely expensive equipment technology prerequisites, and alsoexpensive reagents. These methods can only be carried out by trainedtechnical personnel in special laboratories. On-site diagnostics are notpossible. New generations of integrative system solutions (combinationsof nucleic acid isolation, amplification, and chip detection) for mobileon-site diagnostics are in development, but not in a stage of successfulmarketing. Furthermore, these systems often focus on the sector ofmilitary diagnostics, and, in analogy to the “traditional REAL-TIME PCR”methods, are also very expensive, in terms of both devices and reagents.

The so-called rapid PCR technology allows carrying out amplificationreactions within only a few minutes and is therefore clearly faster thanstandard PCR methods. For the miniaturized device solution, theinvention is accomplished by means of a novel reaction cavity(consumable). In the sector of PCR consumables, various methods areknown for their production. The most widespread is the production methodusing injection-molding. The consumables produced in this manner arecommercially available in a large number of shapes and arrangements.However, these receptacles all have a very thick wall thickness(approximately 0.2 mm-0.35 mm), which opposes good heat transfer fromthe heated sample block into the sample, as a very great resistance. Ifthese receptacles are used as intended, in a thermocycler, the sampleblock situated in the devices heats up at a speed of up to 5° C./s. Theresulting speed in the sample, however, is significantly reduced by thereceptacles, so that the sample (situated in the receptacle) is onlyheated up at approximately 1.5-2° C./s. Even those receptacles offeredfor sale as “thin-wall” receptacles (minimal wall thickness ofapproximately 0.19 mm; Eppendorf product catalog 07-08, p. 200) are notable to significantly improve this condition. The technicalprerequisites (heating and cooling) for rapid processing of thetemperatures in PCR are implemented technically, but the efficacy isgreatly impaired, because of the consumable used.

Usual sample volumes used in PCR lie in the range of 5-50 μl. Thereceptacles, produced by means of injection-molding, possess theirmaximal wall thickness at the bottom, so that tempering andimplementation of a PCR reaction of low volumes, 1-10 μl (which collectat the bottom of the receptacles), can be carried out only veryimprecisely and slowly.

The metallic sample blocks used (aluminum, silver) in thermocyclershaving a very great heat capacity furthermore ensure that rapidtemperature changes in the sample are impossible to implement, even whenusing strong heating elements. The rapidity of existing systems on themarket, which work on the basis of metallic sample blocks andinjection-molded consumables, thus comes up against objective limits.From this, it follows that because of their tremendous thermalinefficiency, miniaturized, mobile variants of these thermocyclersexceed the electrical conductivity of accessible battery technology inunacceptable manner.

Other stationary systems bet on advanced technology to increase thethermal efficiency and make rapid PCR possible.

The most well-known commercially available PCR system that will bementioned here is the LightCycler from Roche Molecular Biochemicals(cat. No. 1909339 and cat. No. 2011468). This system is based on the useof very thin glass capillaries as PCR consumables and carries outtempering by means of hot air that flows around the capillaries. Thesecapillaries can hold a volume of 10-20 μl and are characterized by theirlarge surface area, which allows good heat transfer. However, this largeglass surface area absorbs components of standard PCR batches and thuscauses the reaction to become more and more inactive. In order tocompensate this effect, different carrier molecules, etc., for example,have to be used (EP 1133359). Another disadvantage in this connection isthe handling of the very thin capillaries and their price.Miniaturization and simple handling of the receptacles continues to beimpossible, however.

A technology that is not based on standard consumables and can be usedfor mobile use is explained in the published patent applicationUS2005/0227275 A1. Here, a woven metal textile is introduced into thewall of the PCR reaction chamber, by means of production technology.This ensures direct heat transfer to the sample. Although it is pointedout that the wall should be thin, it is not explained how thin. At thesame time, cooling of the sample is not discussed in any way. Thus,while this reference explains that rapid PCR is supposed to be carriedout, it does not, however, provide sufficient information abouttechnical implementation. This point also includes the fact that theconsumable described there does not meet the requirements of being acost-advantageous consumable material. Introduction of a defined wovenheating material and a device for temperature control stand in the wayof this requirement. Furthermore, the object according to the inventionof the published patent application U.S. 2005/0227275 A1 is furthermorecarrying out a PCR reaction and detecting amplification products bymeans of a lateral-flow strip. PCR with marked primers and nucleotidesis described (claim 1, FIG. 1, 2, 3, 4, 6). However, a disadvantage ofthis method is that the PCR product is not hybridized with a markedprobe. The sole detection of an amplification product in this manner isdiagnostically very uncertain, however, since the required 100%specificity of the amplification product is not guaranteed. For thispurpose, a specific hybridization reaction is required. Furthermore,there is the latent risk that false-positive results occur due tomis-priming and primer dimers.

The use of a design similar to a “chip” for accommodating a PCR chamberdoes not represent level of invention, because it is cited many times inthe patent literature. Instead, the configuration of the heating/coolingmechanism, of the entire heat transfer, the feed of liquid/solidbiochemical reaction components, and the implementation of the processparameter control represent innovation. Thus, for example, the referenceWO 2007/092713 A2 discusses a consumable design in chip form that cancomprise not only cell sorting and immunological protein detection butalso a PCR chamber. Different cell types (precursors of cancer cells,and cancer cells) are separated by means of a lateral-flow test stripmethod, using appropriate antibodies, and discriminated. However, thelateral-flow method does not serve to detect amplification events. Thedetection of RNA expression from RNA, which previously took place in aso-called lab-on-a-chip system, is uncoupled from this lab-on-a-chip andtakes place as described, on a “laboratory table, using known methods.”It is described that alternatively to this, an amplification reactor anda detector can be integral components of the lab-on-a-chip system. Thisreference does not discuss the configuration of the PCR chamber in thesense of the aforementioned properties. There is also no mention of aPCR reaction in the claims. Nevertheless, a mobile variant of theequipment system (with consumable) can be discussed here. For operationof the device independent of the power network, power consumption mustbe optimized and be as low as possible. Because of the use of a largenumber of thermoelectric modules (“hydrogel ice valves”) and fluidpumps, a person skilled in the art recognizes that this device cannot besuitable for mobile battery operation.

The authors of the reference described above discuss the topic of chipproduction and of the PCR chamber within this or a similar chip in apublication (Chen, Z., et al.; Ann. N.Y. Acad. Sci. (March 2007) 1098;429-436). A system is presented that comprises a PCR chamber and alateral-flow test strip. Measured by the requirements—rapid (rapid PCR),mobile (battery operation), cost-advantageous (consumable), and easy tohandle—this invention must be assessed as follows. It is known to anexpert that rapid PCR is defined by the total time of the reaction (with30 cycles in less than 30 minutes) and by the temperature changes in thesample that are achieved (>4 K/second). Without any statement of heatingor cooling rates, a cycle time of at least one minute (sum of the stoptimes without duration of the temperature change), as well as the use ofa PCR chamber made of polycarbonate, produced by means of millingtechnology (wall thickness values of at least 100 μm), it becomes clearto a person skilled in the art that this equipment system cannot be usedfor rapid PCR. In this publication, a mobile system is not described inany manner. Just like in the patent document described above, more than10 thermoelectric modules, plus two multidirectional setting valves, afluid pump, a vacuum pump, and a laser scanner are supposed to beaccommodated here, on the equipment side. These modules, which are verypower-intensive, as well as the consumable design, which is notoptimized, thus preclude even the possibility of mobile batteryoperation. Finally, a person skilled in the art recognizes that thissystem cannot be used for mobile use, since the complexity of theconsumable (multiple production steps, introduction of hydrogels)requires unreasonable production costs. Detection of the amplificationtakes place by way of the use of two marked primers. However, it isknown to a person skilled in the art that such a detection method on atest strip is highly problematical, since specific amplificationproducts cannot be separated from the non-specific amplificates andso-called primer dimers. Thus, such a detection system cannot be used indiagnostics.

Furthermore, the publication by Wang et al. belongs to the state of theart (Wang, J. et al.; Lab on a Chip (2006) 6: 46-53. The systempresented there can be identified by a person skilled in the art as avariant of the two developments described above (for example the sameuse of ice valves or marked primers as a detection system). Here, theprecise properties of the PCR reaction unit are stated once more inconcrete terms. A thickness of 250 μm is indicated for the wall betweenthe heating/cooling element and the sample. On the technology side, thischamber and all the channels are introduced into a polycarbonate carrierby means of a CNC milling process. Therefore, the thermal resistance ofthis chamber still lies above that of commercially available reactionreceptacles (wall thickness 200 μm to 300 μm; material polyethylene), inwhich rapid PCR is only possible by means of high-power equipment. Thus,use of the concept for battery operation is excluded once again. Theinefficiency of the concept becomes evident to a person skilled in theart when the authors discuss the difficulties in achieving an acceptablecooling rate. Even with active heat transport by means of Peltierelements and the inclusion of a 14 watt fan (conventional fans forprocessors require 6 watts), only 2.6 K/second is achieved in the sample(see rapid PCR). The concept must also be critically illuminated withregard to the formulated goal of cost minimization. According to thepublication, many different production chains have to be run through inorder to produce a chip with this concept. Aside from milling of theprecision channels, the surfaces additionally have to be polished,hydrogels have to be introduced, two chip halves have to be joined,using a complicated thermal method, and subsequently, reactivation ofthe gels has to be implemented. This makes it evident to a personskilled in the art that this chip concept makes a cost-advantageousconsumable impossible.

BRIEF DESCRIPTION OF THE INVENTION

The invention was based on the task of developing a novel mobilegene-diagnostic rapid test system (combination of hardware andreagents), which is supposed to be easy to operate, allows extremelyrapid diagnostic information, and is inexpensive both with regard to thedevice and with regard to the test to be performed. Therefore, thepossibility of being able to carry out diagnostics of infectiousdiseases in developing countries, without qualitative restrictions, isalso supposed to be created.

The mobile rapid test system, according to the invention, for nucleicacid analysis comprises a device for amplification and hybridization ofnucleic acids, with amplification primers and at least one hybridizationprobe, as well as a test kit for detection of the amplification event,and is characterized in that

a) the amplification product and the hybridization probe contain atleast one marker, in each instance, andb) the test kit comprises at least one lateral-flow test strip, whichcontains a zone for coupling the markers, in each instance.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be explained in greater detail using two figures. Inthe appendix, the fundamental diagrams for the means according to theinvention are shown. In this connection, the drawings are not considereda limitation for other embodiments.

FIG. 1 shows the schematic representation of the cartridge.

FIG. 2 shows the schematic representation of the device (voltage sourceand reaction cartridge).

REFERENCE SYMBOL LIST

-   A: Inlet opening-   B: Consumable for the amplification/hybridization reaction-   C: Outlet opening and connection between consumable and test strip-   D: Reservoir for running buffer-   E: Outlet opening from reservoir for running buffer, with feed to    the test strip-   F: Test strip-   G: Viewing window for detection of the detection signal on the test    strip-   H: Battery as a voltage source-   I: Heating/cooling element

DETAILED DESCRIPTION OF THE INVENTION

The term “marker” is understood to mean any atom or molecule that can beused to generate a detectable (preferably quantifiable) signal on alateral-flow test strip, and that can be bound to a nucleic acid.

Markers can preferably generate signals by means of fluorescence,colorimetry, or enzymatic activity. Markers by means of biotin and FITC(fluorescein isothiocyanate) are preferred.

Marking of the amplification product takes place either by means ofmarking of a primer or from marking of the nucleic acid to bedetermined.

The devices and the test kit are integral components of the mobile rapidtest system, and this system represents a miniaturized, mobile-operated,hand-held device that requires no external voltage source duringoperation, but rather is operated by means of a battery or arechargeable battery.

Mobile rapid test system contains a reaction cavity for carrying outamplification of nucleic acids, preferably by means of rapid PCRtechnology, one or more inlet and/or outlet openings for the reactioncavity, one or more heatable sample blocks that are connected withminiaturized cooling bodies, and a possibility for reading off theresult, whereby the reaction cavity contains a plastic film having afilm thickness that is less than 300 μm, preferably less than 250 μm,200 μm, 150 μm or 100 μm. These film thickness values include allintermediate values and subranges. The plastic film preferably consistsof polypropylene, and is welded, with a stable shape, in a desiredgeometry, and pressed onto the sample block with light contact pressure,from above.

An amplification primer is preferably marked by means of biotin, and thehybridization probe is preferably marked with FITC, and is protected(“blocked”) against polymerization at the 3′ end. This “blocking” can beachieved, for example, by using non-complementary bases or by adding achemical group, such as a phosphate group, at the 3′-hydroxyl of thelast nucleotide. Blocking can also be achieved by removing the 3′-OH orby using a nucleotide without the 3′-OH, such as a dideoxy nucleotide.

The lateral-flow test strip carries separate binding locations,preferably two, a streptavidin location for coupling the markedamplification products, and a binding location for function monitoringof the test strip, as well as a zone with conjugated detection particles(for example anti-FITC gold particles).

The object of the invention is also a method for detection of nucleicacids by means of the mobile rapid test system described above, havingthe following steps:

-   -   Amplification of the nucleic acids by means of the rapid PCR        technology, with amplification primers, of which either at least        one is marked or the nucleic acids were marked,        -   Conversion of a double-strand amplification product into a            single-strand DNA fragment (denaturing),        -   Hybridization of the denatured amplification product with at            least one marked hybridization probe,        -   Detection of the nucleic acids on a lateral-flow test strip,            which contains a zone for coupling of the markers, in each            instance.

The invention solves the problems described in ideal manner, by means ofthe simple and synergistic combination of an equipment system forcarrying out specific amplification reactions and simple detectionchemistry for detection of a specific amplification event, whereby theequipment system is present in the form of a so-called hand-held system,and this is not only miniaturized but also can be operated in mobilemanner, i.e. without the need for an external voltage source,particularly by means of battery operation.

In this connection, the invention is based on the use of the so-calledrapid PCR technology.

The invention solves the existing problems of a miniaturized, hand-heldrapid PCR thermocycler in combination with a detection model as follows:

The invention is based on a novel arrangement and concept of heatingelements and sample block, which are suitable for mobile use in terms ofpower and size, in combination with a completely novel consumable(reaction cavity for the amplification reaction) having a significantlyimproved heat transfer. This is achieved, according to the invention, inthat the novel consumable is optimized in such a manner that the biggestproblem, the physical resistance for effective PCR tempering, can beovercome. An optimal heat transfer is present when a sample can beapplied directly to the sample block or tempered medium, withoutinterfering materials and additional heat transfers. Such implementationhas been impossible up to now for reasons of contamination.

Only minimal interference of the heat transfer would exist if anextremely thin layer of a biocompatible material could be used. This issolved, according to the invention, in that an extremely thin-layered PPfilm is used. In this connection, this film is laid or folded into adesired geometry, and welded in stable shape. This specific geometry ischaracterized in that it possesses the largest possible flat surfacearea at the bottom, for the sample volume of the amplification batch tobe filled in. This large surface area serves as a heat transfer surfaceto the heated sample block. Because of the ultra-thin film, minimalresistance to the heat transfer takes place. All non-heated surfaces ofthe reaction chamber are reduced to a minimum, so that no unnecessaryheat flow to the surroundings can take place. Thus, it is possible toimplement a heating rate effectiveness from the sample block to thesample of almost 100%, within the sample.

Preferably, the non-heated surface areas are <1.4, 1.4, 1.5, 1.6, 1.7,1.8, 1.9, 2.0 or >2.0 times larger, particularly 1.7 times larger, thanthe heated surface areas.

A Peltier element operated by a battery is used as the sample block tobe used; it is screwed onto a cooling body adapted to the system as awhole. The geometry of the sample block that is used is alsocharacterized by a maximal surface area, as a counterpart of theconsumable. The volume and thus also the capacity of the sample blockare reduced to an absolute minimum, according to the invention.Therefore the sample block can theoretically be heated at a heating rateof 15° C./s. The geometry of the consumable has been selected to be solarge, according to the invention, that strong contact pressure onto thesample block is implemented by means of slight downward pressure fromabove and physical effects that are utilized and therefore uniformheating at these speeds is also promoted and implemented in this way.

Thus the prerequisites for implementing an amplification reaction with asmall, mobile device, using a normal battery, and carrying out anultra-rapid reaction, have been created. However, it is clear to aperson skilled in the art that mobile on-site diagnostics cannot becarried out solely with a miniaturized and mobile possibility ofimplementing the PCR reaction. For this purpose, the system alsorequires detection of a specific target amplification that has takenplace.

In this connection, the detection must be an integral component of thesystem as a whole. This combination of amplification and detection issurprisingly implemented in very simple manner, according to theinvention, by means of the use of so-called lateral-flow strips that areknown to a person skilled in the art. Although the two technologies(rapid PCR and lateral-flow strips) exist as standard techniques, thereis no link between the two technologies in the form of an integrativeoverall system that fulfills the requirements for a specific diagnosticsystem. As has already been explained, a number of similar equipmentsystems use detection strategies that do not allow correct diagnosticsor do not use an amplification reaction of nucleic acids (U.S.2005/0227275 A1, WO 2007/092713 A2, Chen, Z., et al.; Ann. N.Y. Acad.Sci. (March 2007) 1098: 429-436, Wang, J. et al.; Lab on a Chip (2006)6: 46-53).

However, precise diagnostics are made possible by the invention.Therefore the invention not only combines an amplification module with alateral-flow strip, but also is based on a detection strategy that takesthe diagnostic requirements into account. To underline the differences,it will be emphasized once again, in the following, how lateral-flowstrips are used for DNA/RNA diagnostics.

Carrying out gene tests by means of so-called lateral-flow strips hasbeen propagated in different forms up to now. One possibility (publishedpatent application KR 1020060099022 A; Method for the detection andanalysis of nucleotide sequence using membrane lateral flow, and kit forsame) used lateral-flow methods for detecting nucleic acids. This methoduses the technology of hybridization of nucleic acids on a solid phase.In this connection, specific captor nucleic acids are immobilized on thetest strip and hybridized with single-strand target nucleic acids. Acaptor nucleic acid is a single-strand ribonucleic acid ordeoxyribonucleic acid, or one that only becomes single-strand during thecourse of the process, which possibly contains chemically modified basesor base analogs, chemically modified sugars or sugar analogs, or ismodified in some other way, and is characterized in that it binds to aspecific, predetermined nucleic acid or class of nucleic acids at highspecificity and selectivity. In this connection, this process requiresthe conversion of a double-strand DNA fragment (as the result of aspecific amplification reaction) into a single-strand DNA fragment. Forthis purpose, the process must be carried out subsequent to a PCRreaction. Another rapid detection method that also uses the detection ofamplification products by means of a test strip and is availablecommercially is based on a completely different principle, in contrastto the above patent document. Here, implementation of the PCR reactionis carried out with a biotinylated primer and a non-biotinylated primer.After the PCR is carried out, a PCR product is present, which isbiotin-marked at one end. The detection uses a test strip (for examplefrom Millenia), which contains two separate binding locations. Astreptavidin location for coupling the biotin-marked DNA strand and anFITC binding location for monitoring the function of the test strip.

The detection of the PCR product is implemented in that after PCR hasbeen carried out, the PCR batch is denatured and hybridized with a probethat is complementary to the biotin-marked DNA strand. The probe isFITC-marked.

For detection, the PCR batch is mixed with a running buffer and appliedto the test strip. According to the test description, the biotinylatedDNA strand binds to the streptavidin binding location of the strip.Detection takes place by way of the FITC marker of the probe hybridizedwith the DNA strand. A typical signal is formed, in the shape of astrip. This signal is supposed to be the specific detection of theamplification product. However, the method does not combinehybridization of the probe with the process of PCR, but rather carriesthis out as a separate method step. However, the method has afundamental and dramatic error source.

The detection of the target nucleic acid to be detected is not specific.The cause for this lies in the fact that artifacts that were formedduring PCR, for example primer dimers, of course also bind specificallyto the streptavidin binding location of the test strip, and thereforecan cause a positive reaction, just like a specific PCR product (asalready described multiple times in the above text).

From these explanations, it follows that while there are applicativesolutions for carrying out gene tests on strips, these require not onlyamplification but also denaturing of the amplification product, and thusdo not permit a direct combination of amplification and detection.Furthermore, as shown in Example 2, certain methods are not specific,and are very problematical with regard to the production offalse-positive diagnostic results.

A novel and very elegant possibility is based on a probe hybridizationbetween amplificate and specific hybridization probe that is integratedinto the amplification reaction. The detection of the specifichybridization event then takes place on a test strip.

In this way, the possibility is created, for the first time, of workingwithout further manipulation (denaturing of double-strand DNA) andcircumventing the amplification problems that have already beenpresented, and thus of being able to combine theamplification/hybridization reaction directly with detection on a teststrip. Detection of an amplification/hybridization product takes placein that an amplification primer and the specific hybridization probe atthe 3′-end are provided with a marking molecule, in each instance (forexample biotin and FITC). The amplification reaction takes place understandard conditions. In this connection, the actual amplificationreaction is followed by a denaturing step for thermal strand separationof the amplification product generated during PCR. After denaturing, thePCR reaction batch is cooled to the hybridization temperature of theprobe. During this step, the hybridization probe binds specifically tothe complementary DNA strand of the amplification product. In thisconnection, this strand carries the biotin marker that was installed inthe PCR product by means of the biotin-marked primer. After theamplification/hybridization reaction has been carried out, the reactionbatch is transferred to the test strip. On this test strip, detection ofthe specific hybridization event can take place as follows: The teststrip carries two separate binding locations, for example, in oneembodiment variant; a streptavidin location for coupling thebiotin-marked amplification products, and an FITC binding location formonitoring the function of the test strip. Furthermore, the test stripcontains a zone with conjugated detection particles (for exampleanti-FITC gold particles). After the PCR batch is brought into contactwith such a test strip, the following binding events can occur:

-   -   1. All the FITC-marked nucleic acids (non-hybridized FITC-marked        hybridization probe and/or hybridization product between        biotin-marked DNA strand and FITC-marked hybridization probe)        bond to gold particles that are coated with anti-FITC        antibodies, in the lower sample application region of the test        strip.    -   2. In the further progression of the test strip, there is the        streptavidin binding location. The following nucleic acids can        bind to this binding location:        -   (a) the biotin-marked primers,        -   (b) the biotin-marked DNA strands, and        -   (c) the hybridization products between biotin-marked DNA            strand and FITC-marked hybridization probe.

However, a detection signal can only become visible if the specifichybridization product between biotin-marked DNA strand and FITC-markedhybridization probe is present, since only this product is also coupledwith the detection system (FITC/anti-FITC gold particles).

-   -   3. In the further progression of the test strips, excess gold        particles coated with anti-FITC antibodies then also bind; these        serve as a control to check the ability of the test strip to        function.

This embodiment variant, as has already been mentioned, is very elegantand does not entail the potential risk of false-positive signals. It istherefore the variant to be preferred for use of a lateral-flow teststrip, for the mobile detection system according to the invention.

The invention should be understood as a combination of the novel methodfor detection of amplificates and a novel device for mobile use. In theimplementation of the device according to the invention, the detectionstrategy by means of lateral-flow strips, intelligent sampleapplication, and energy-efficient tempering of sample volumes arecombined, to produce a consumable that is cost-advantageous because itis simple to produce.

An embodiment of the device according to the invention looks as follows:

The consumable represents a design integration of the functional modulesfor application of the reaction mixture initially produced (nucleic acidto be investigated, dNTPs, primer, hybridization probe, as well asamplification buffer), for implementation of an energy-efficientamplification reaction, for storage and application of a running buffer,as well as for the detection reaction by means of test strips. Thebattery-operated device is configured in such a manner that itrepresents an ideal means for processing the functional sections of theconsumable. The sequence of processing begins with application of thereaction mixture by way of the inlet opening, whereby the mixture isguided into the amplification chamber directly or by way of additionalprocess segments. After the amplification/hybridization reaction hastaken place, the reaction batch is transferred to the test strip by wayof the outlet opening. Subsequently, the running buffer is also passedto the test strip, from a separate reservoir, whereby in one embodimentvariant, the running buffer can first pass through the reaction chamber.The reservoir for the running buffer is also situated in the cartridge.After the test strip reaction has been completed, the diagnostic resultis read off in a viewing zone. The reaction cartridge, which containsthe amplification module and the test strip, as well as the reservoirfor the running buffer, is preferably a disposable article, in otherwords, a new one is inserted into the base device for every reaction anddisposed of after the test has been run.

The device according to the invention is an object of the inventiondescribed, even without the detection system according to the invention,and can also be combined with the detection system for captor nucleicacids that was mentioned above. In this way, a system is made availablethat consists of the device according to the invention, according to theembodiments described herein, and a test strip on which special captornucleic acids are immobilized, and with which detection of the nucleicacids to be determined takes place by means of hybridization with thecaptor nucleic acids on the test strip. Preferably, such a system willcomprise a device that is a miniaturized hand-held device that can beoperated in mobile manner, which does not require any external voltagesource during operation, but rather is operated by means of a battery ora rechargeable battery, and which integrates said device and said testkit. The hand-held device can comprise a reaction cavity for carryingout an amplification of nucleic acids by means of the rapid PCRtechnology, one or more inlet and/or outlet openings for the reactioncavity, one or more heatable sample blocks that are connected withminiaturized cooling bodies, and a means for reading the result, whereinthe reaction cavity contains a plastic film having a film thickness thatis less than 300 μm, preferably a film thickness of less than 100 μm.The plastic film may consist of polypropylene and is welded in a desiredgeometry, in shape-stable manner, and is pressed against the sampleblock by means of slight contact pressure from above. The reactioncavity and the test strip can be disposed in a reaction cartridge, andthe plastic film produces connection channels with the reactioncartridge. The system may further comprise a reservoir and an outletopening for running buffer or contain connection channels between areaction cavity, test strip, and running buffer reservoir, which can beclosed off. The reaction cavity may have two surfaces that can beconnected with one another at channel or chamber edges, with force fitand/or shape fit, whereby at least one of these surfaces consists of aplastically or elastically deformable material. The reaction cavity canalso comprise a depression and the sample block can be configured inconvex manner with the chamber opening being circular. This system maycontain reaction cavity that contains movable pistons and related hollowcylinders for storage of reactants. It may also comprise a heatablesample block, which is connected with a miniaturized cooling body, thatcontains a battery-operated Peltier element having a heating rate of <5°C./s, 5° C./s, 10° C./s, 12.5° C./s and up to 15° C./s.

In the following, these embodiment variants according to the inventionwill be explained, without restricting the invention to these variants.

EXEMPLARY EMBODIMENTS Example 1

The reaction mixture is fed into the inlet opening. The inlet opening iswelded shut by means of a heated wire that is integrated into thedevice. In this connection, the heated wire is moved to the inletopening by means of a simple pressure mechanism. In this embodiment,both the consumable used for the amplification/hybridization reaction,according to the invention (reaction cavity), and the test strip areplaced in a reaction cartridge, one behind the other.

Example 2

The embodiment variant of the consumable is structured in such a mannerthat one or all the fluids on the consumable are transported from onefunctional module to the next by way of novel fluid structures. Thesestructures are produced by means of production technology, in that twosurfaces are applied to one another, whereby at least one of thesesurfaces consists of a plastic or elastically deformable material. Atthe delimitations of the structures, for example the edges of thechannels or chambers, the two surfaces are connected with one another,by means of force fit and/or shape fit. When fluid pressure is appliedto the small gap that this structure can represent, then at least one ofthe surfaces domes up and releases a larger gap for passage between thetwo surfaces. By means of this novel concept, cost-advantageousproduction of fluidic elements on the consumable is made possible.

Example 3

In another embodiment variant, the reaction chamber represents aperforation or depression in the carrier material of the consumable.Closure of the chamber is achieved in that the film that lies on top ofit is pressed against the edges of the perforation or depression. In anembodiment of this variant, the pressure is produced by the sampleblock, so that the latter brings about not only the heat transfer butalso the chamber closure. The increased demands on the pressure sealduring PCR are achieved in that the sample block is configured in convexmanner and the chamber opening is circular.

Example 4

Storage and application of the running buffer can be configured asfollows, in one embodiment variant: A cavity is created between the filmand the carrier material, by means of production methods that create aspace. This cavity is filled with running buffer duringproduction/outfitting of the consumable. The outlet opening of thereservoir is closed off with a pressure-dependent valve, which can beimplemented, for example, by means of a welding seam that can bere-opened. In order to feed the buffer into the reaction chamber, thebuffer chamber has pressure applied to it, by the device or by the user,in such a manner that the valve opens and the buffer is moved to thetest strip.

Example 5

In this embodiment variant, movable pistons and related hollow cylindersare part of the consumable. In this connection, these cylinders can befilled with fluid on the production side (for example running buffer,reactants). The inlet opening of the consumable is shaped in such amanner that a sample application tool can be connected in shape-fitmanner. This tool is also composed of a hollow cylinder that has apiston. For sampling, the piston is pulled up into the cylinder and thenconnected with the consumable. The pistons of the consumable and of thesampling tool can be moved by the user or by the device. The sample ispressed into the reaction chamber by means of the piston movement at thesample application tool. Air that has to be displaced from the chamberor from the fluidic regions in this manner escapes into the air-freespaces and/or out of the outlet openings that are fluidically situatedbehind the detection region. Then, one or more sample blocks are presseddown from one or more sides of the reaction chamber. With this process,the reaction chamber is sealed in airtight manner, as in Example 4, sothat energetically advantageous tempering of the sample can take place.When the sample blocks are removed, the sample can now be pressedfurther in the direction of the detection chamber. For this purpose, thepiston of the sample application tool and/or the piston of the cylinderwith the running buffer can be moved. Air and/or fluids from thecylinders described displaces the sample from the reaction chamber andmoves it toward the test strip. Additional running buffer from thecorresponding cylinder is applied to the test strip by means of themovement of the pistons. The user can read off the result of thedetection by way of a viewing window in the detection region. In anotherembodiment variant, the detection region, just like the applicationtool, can be reversibly removed from and connected with the consumableas a whole, and can be replaced by an alternative detection system.

With the combination of rapid PCR and detection of the amplificationevent according to the invention, by means of a mobile andbattery-operated hand-held system, the prerequisites for very simple andinexpensive gene-diagnostic on-site analysis have been created for thefirst time. In this connection, of course, the hand-held device is muchless expensive than the previously proposed high-technology equipmentsystems, particularly for military applications. This is also supposedto universally allow use of gene-diagnostic rapid tests in developingcountries. By means of the method according to the invention, it is madepossible to carry out an extremely rapid amplification reaction. Thesubsequent detection on a test strip is also very fast and robust. Thus,the invention represents a real rapid test system.

Various modifications and variations of the described systems, devices,primers, probes, markers, other system elements, and methods of theirconfiguration and use as well as the concept of the invention will beapparent to those skilled in the art without departing from the scopeand spirit of the invention. Although the invention has been describedin connection with specific preferred embodiments, it should beunderstood that the invention as claimed is not intended to be limitedto such specific embodiments. Various modifications of the describedmodes for carrying out the invention which are obvious to those skilledin the medical, biological, chemical or pharmacological arts or relatedfields are intended to be within the scope of the following claims.

Each document, patent, patent application or patent publication cited byor referred to in this disclosure is incorporated by reference in itsentirety, especially with respect to the specific subject mattersurrounding the cited reference. However, no admission is made that anysuch reference constitutes background art and the right to challenge theaccuracy and pertinency of the cited documents is reserved.

1. A mobile rapid test system for analysis of a nucleic acid to bedetermined, comprising: a device for amplification and hybridization ofnucleic acids, amplification primers optionally comprising at least onemarker, at least one hybridization probe comprising at least one marker,and a test kit for detection of an amplification event that comprises atleast one lateral-flow test strip having a zone for coupling markers. 2.The mobile rapid test system according to claim 1, further comprising anucleic acid to be determined.
 3. The mobile rapid test system accordingto claim 1, further comprising a nucleic acid to be determined that ismarked.
 4. The mobile rapid test system according to claim 1, whereinthe amplification primers comprise a marker.
 5. The mobile rapid testsystem according to claim 1, further comprising a marked nucleic acidproduced from the nucleic acid to be determined.
 6. The mobile rapidtest system according to claim 1, which comprises a hand-held devicethat can be operated in mobile manner, which does not require anyexternal voltage source during operation, but rather is operated bymeans of a battery or a rechargeable battery, and which integrates saiddevice and said test kit.
 7. The mobile rapid test system according toclaim 6, wherein the hand-held device comprises a reaction cavity forcarrying out an amplification of nucleic acids by means of the rapid PCRtechnology, one or more inlet and/or outlet openings for the reactioncavity, one or more heatable sample blocks that are connected withminiaturized cooling bodies, and a means for reading the result, whereinthe reaction cavity contains a plastic film having a film thickness thatis less than 300 μm.
 8. The mobile rapid test system according to claim7, wherein said plastic film as a film thickness of less than 100 μm. 9.The mobile rapid test system according to claim 7, wherein the plasticfilm consists of polypropylene and is welded in a desired geometry, inshape-stable manner, and is pressed against the sample block by means ofslight contact pressure from above.
 10. The mobile rapid test systemaccording to claim 7, wherein the reaction cavity and the test strip aredisposed in a reaction cartridge and the plastic film producesconnection channels with the reaction cartridge.
 11. The mobile rapidtest system according to claim 1, further comprising a reservoir and anoutlet opening for running buffer.
 12. The mobile rapid test systemaccording to claim 1, which contains connection channels between areaction cavity, test strip, and running buffer reservoir, which can beclosed off.
 13. The mobile rapid test system according to claim 1,comprising a reaction cavity that contains two surfaces that can beconnected with one another at channel or chamber edges, with force fitand/or shape fit, whereby at least one of these surfaces consists of aplastically or elastically deformable material.
 14. The mobile rapidtest system according to claim 1, comprising a reaction cavity thatcontains a depression and the sample block is configured in convexmanner and the chamber opening is circular.
 15. The mobile rapid testsystem according to claim 1, comprising a reaction cavity that containsmovable pistons and related hollow cylinders for storage of reactants.16. The mobile rapid test system according to claim 1, comprising aheatable sample block, which is connected with a miniaturized coolingbody, that contains a battery-operated Peltier element having a heatingrate of up to 15° C./s.
 17. The mobile rapid test system according toclaim 1, wherein an amplification primer and the hybridization probe aremarked at the 5′-end.
 18. The mobile rapid test system according toclaim 17, wherein the amplification primer is marked by means of biotinand the hybridization probe is marked by means of FITC, and protectedagainst polymerization at the 3′-end.
 19. The mobile rapid test systemaccording to claim 1, wherein the lateral-flow test strip carries twoseparate binding locations, a streptavidin location for coupling of themarked amplification products, and a binding location for monitoring thefunction of the test strip, as well as a zone with conjugated detectionparticles (for example anti-FITC gold particles).
 20. A method fordetection of nucleic acids by means of the mobile rapid test systemaccording to claim 1, comprising: amplifying of the nucleic acids bymeans of the rapid PCR technology, with amplification primers, of whicheither at least one is marked or the nucleic acids were marked,converting of a double-strand amplification product into a single-strandDNA fragment (denaturing), hybridizing of the denatured amplificationproduct with at least one marked hybridization probe, detecting of thenucleic acids on a lateral-flow test strip, which contains a zone forcoupling of the markers, in each instance.
 21. The method according toclaim 20, wherein the PCR reaction is carried out with a marked primerand an unmarked primer for each DNA fragment to be detected, in eachinstance, and the test strip contains a binding location for the markerof the primer, in each instance, whereby the detection of the nucleicacids takes place in that the denatured amplification product ishybridized with a marked probe that is complementary to the DNA strandmarked with the primers, the PCR batch is mixed with a running bufferand applied to the test strip.
 22. The method according to claim 20,wherein after denaturing of the PCR reaction batch, cooling to thehybridization temperature of the probe takes place, whereby thehybridization probe specifically binds to the complementary DNA strandof the amplification product and this DNA strand carries the biotinmarker that was installed into the PCR product by the biotin-markedprimer.